人妻少妇偷人精品无码丨色婷婷av久久久久久久丨欧美xxxx做受性欧美88丨欧洲女人牲交视频免费丨亚洲精品久久久av无码专区

熱門搜索:A549    293T 金黃色葡萄球菌 大腸桿菌 AKK菌
購物車 1 種商品 - 共0元
當前位置: 首頁 > ATCC代理 > SR-4987
最近瀏覽歷史
聯系我們
  • 0574-87157013
  • mingzhoubio@163.com
  • 浙江省寧波市鎮海區莊市街道興莊路9號
  • 創e慧谷42號樓B幢401室
SR-4987
SR-4987
規格:
貨期:
編號:B165752
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規格:
凍干粉
斜面
甘油
平板


產品名稱 SR-4987
商品貨號 B165752
Organism Mus musculus, mouse
Tissue bone marrow
Cell Type virus transformed
Product Format frozen
Morphology fibroblast
Culture Properties adherent
Biosafety Level 2

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Disease Leukemia
Age 5 months
Gender female
Strain BDF1
Applications
transfection host
Storage Conditions liquid nitrogen vapor phase
Karyotype tetraploid
Derivation
The SR-4987 cell line was established by treating normal marrow cells with supernatant from Y-1 cells (known to produce Murine Leukemia Virus (MuLV).
Clinical Data
female
Genes Expressed
macrophage colony stimulating factor (MCSF)
Cellular Products
macrophage colony stimulating factor (MCSF)
Tumorigenic Yes
Effects
Yes, produce sarcomas in syngeneic mice
Comments
The SR-4987 cell line was established by treating normal marrow cells with supernatant from Y-1 cells (known to produce Murine Leukemia Virus (MuLV).
The cells produce MCSF, and are highly sensitive to fibroblast growth factor (FGF).
They are poorly clonogenic in soft agar.
Neither interleukin 3 (IL-3) or granulocyte colony stimulating factor (GCSF) were detected in SR-4987 conditioned medium.
Complete Growth Medium The base medium for this cell line is ATCC-formulated McCoy's 5a Medium Modified, Catalog No. 30-2007. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin-0.53mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
  3. Add 2.0 to 3.0 mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
    Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 37°C.

Subcultivation Ratio: 1:4 to 1:8
Medium Renewal: Every 2 to 3 days

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a Manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.

Cryopreservation

Complete growth medium described above supplemented with 5% (v/v) DMSO.  Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions
Temperature: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Population Doubling Time 15 hrs
Name of Depositor G Zaleskis
Deposited As Mus musculus
References

Pessina A, et al. Establishment and characterization of a new murine cell line (SR-4987) derived from marrow stromal cells. Cytotechnology 8: 93-102, 1992. PubMed: 1382506

Pessina A, et al. Expression of B cell markers on SR-4987 cells derived from murine bone marrow stroma. Exp. Hematol. 25: 536-541, 1997. PubMed: 9197333

Pessina A, et al. Role of SR-4987 stromal cells in the modulation of doxorubicin toxicity to in vitro granulocyte-macrophage progenitors (CFU-GM). Life Sci. 65: 513-523, 1999. PubMed: 10462078

Hay, R. J., Caputo, J. L., and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC.

Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988.

Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC.

梅經理 17280875617 1438578920
胡經理 13345964880 2438244627
周經理 17757487661 1296385441
于經理 18067160830 2088210172
沈經理 19548299266 2662369050
李經理 13626845108 972239479
主站蜘蛛池模板: 自慰无码一区二区三区| 扒开双腿猛进入喷水高潮视频 | 精品麻豆国产色欲色欲色欲www| 五月色婷婷丁香无码三级| 丰满少妇大力进入| 欧美老妇大p毛茸茸| 2020精品国产自在现线看| 国产美足白丝榨精在线观看sm| 好硬好湿好爽好深视频| 欧美日本日韩| 亚洲人亚洲精品成人网站| 亚洲无线看天堂av| 亚洲制服丝袜自拍中文字幕| 亚洲hdmi高清线| 国产亚洲精品久久久久婷婷瑜伽 | 国产偷久久久精品专区| 经典三级欧美在线播放| 两口子交换真实刺激高潮| 久久久久久国产精品免费免费男同| 真人做受试看120分钟小视频| 九九久久精品国产免费看小说 | 国产免费又爽又色又粗视频| 亚洲乱码一区二三四区ava| 国产免费人成网站x8x8| 国产精品99久久久久久宅男| 亚洲中文字幕无码中文字在线 | 亚洲精品国产suv一区88| 大陆熟妇丰满多毛xxxⅹ| 在线观看国产午夜福利片| 久久99精品国产99久久6男男| 日韩av无码中文无码不卡电影| 国产精品18久久久| 免费人成激情视频在线观看| 蜜臀av性久久久久蜜臀aⅴ麻豆| 国产老妇伦国产熟女老妇视频| 亚洲系列一区中文字幕| 久久天天躁夜夜躁狠狠躁| 国产精品视频| 久久人人爽人人爽人人片dvd| 国产黑色丝袜视频在线观看网红| 国产又粗又猛又黄又爽无遮挡 |